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SNP Report
Name | rs8057847 dbSNP Ensembl | ||
---|---|---|---|
Location | chr16:19524216 - 19524216(1) | ||
Variant Alleles | T/A/C | ||
Ancestral Allele | T | ||
Minor Allele | C | ||
Minor Allele Frequence | 0.15595 | ||
Functional Annotation | intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000381396, ENST00000396212, ENST00000562083, ENST00000565376, ENST00000569190, ENST00000573412); NMD_transcript_variant(ENST00000562083); non_coding_transcript_variant(ENST00000569190, ENST00000573412); upstream_gene_variant(ENST00000353258, ENST00000396208, ENST00000561888, ENST00000564172, ENST00000569773) | ||
No. of Studies | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |